CONTRACT- Clinical Trial Management Associate

Position: Clinical Trial Management Associate

Contract: 12 Months 

Location: London (Remote Working)

Umbilical Life is working with a Pharmaceutical client to source an experienced Clinical Trial Management Associate, experienced across the clinical trial phases 

• The CTMA will be responsible working across multiple studies from start-up to close-out activities.
• Working closely with the CPM and vendors, you will involved in site selection and study implementation as well as coordinating these study sites.
• You will ensure SOPs, protocol procedures and regulatory documents reviews are all adhered to. 
• Review of CRO/Vendor trip reports.
• Protocol review, crfs, study plans, monitoring plans, study plans, and clinical study reports..

Qualifications & Experience:

• Educated to degree level in a scientific discipline or equivalent.
• Experience previously as a CRA.
• Knowledge of post-marketing requirements and different types of post-authorisation safety and efficacy studies.
• Must be able to generally understand, interpret, and explain protocol requirements to others.
• Good knowledge and understanding of ICH GCP, GVP, FDA and EMEA regulations and guidelines applicable to post-authorization studies.
• Must be able to prioritize multiple tasks.
• Must be able to participate in multiple departmental or interdepartmental strategic initiatives under limited supervision.
• Must be able to resolve problems using national and international regulations, guidelines, and investigator interaction.

Reference ID: 18545